Rahul V. Tikale , Abhijeet R. Kadam , Ashish Mathur , S.J. Dhoble
{"title":"Sm3+ activated Ba3LaNa(PO4)3F fluorophosphate phosphor: Synthesis, characterization and their photoluminescence investigation for warm WLEDs","authors":"Rahul V. Tikale , Abhijeet R. Kadam , Ashish Mathur , S.J. Dhoble","doi":"10.1016/j.chphi.2024.100741","DOIUrl":null,"url":null,"abstract":"<div><div>In this present research report, the series of Ba<sub>3</sub>LaNa(PO<sub>4</sub>)<sub>3</sub>Fphosphor doped with Sm<sup>3+</sup> was successfully synthesized by using a high-temperature solid-state reaction method. The phase purity was examined using X-ray diffraction (XRD), which confirmed a pure phase of prepared material after sintering the sample at 700 °C. Fourier transform infrared (FT-IR) spectra showed absorption bands corresponding to the stretching and vibrational modes of PO<sub>4</sub> in phosphate. Scanning electron microscopy (SEM) images displayed the morphology of sample and agglomerated structure of micron-sized particles. Photoluminescence excitation (PLE) and emission spectra of the Ba<sub>3</sub>LaNa(PO<sub>4</sub>)<sub>3</sub>F: Sm<sup>3+</sup> phosphors were studied. When excited with near-UV light, the phosphor showed three prominent peaks at 567, 604, and 643 nm. The emission spectra for different concentrations of Sm<sup>3+</sup> ions were also measured to find the optimal dopant concentration. The highest intensity was observed at a 2.0 mol% concentration of Sm<sup>3+</sup> ions at 604 nmwith concentration quenching occurring beyond this point. The CIE chromaticity coordinates for the different concentration phosphor were located in the orange-red region, indicating its characteristic light emission. So therefore, these results suggested that the synthesized reddish-orange light-emitting Ba<sub>3</sub>LaNa(PO<sub>4</sub>)<sub>3</sub>F: Sm<sup>3+</sup>prepared phosphor is promising for applications in white light-emitting diodes (WLEDs).</div></div>","PeriodicalId":9758,"journal":{"name":"Chemical Physics Impact","volume":null,"pages":null},"PeriodicalIF":3.8000,"publicationDate":"2024-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Physics Impact","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667022424002858","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
In this present research report, the series of Ba3LaNa(PO4)3Fphosphor doped with Sm3+ was successfully synthesized by using a high-temperature solid-state reaction method. The phase purity was examined using X-ray diffraction (XRD), which confirmed a pure phase of prepared material after sintering the sample at 700 °C. Fourier transform infrared (FT-IR) spectra showed absorption bands corresponding to the stretching and vibrational modes of PO4 in phosphate. Scanning electron microscopy (SEM) images displayed the morphology of sample and agglomerated structure of micron-sized particles. Photoluminescence excitation (PLE) and emission spectra of the Ba3LaNa(PO4)3F: Sm3+ phosphors were studied. When excited with near-UV light, the phosphor showed three prominent peaks at 567, 604, and 643 nm. The emission spectra for different concentrations of Sm3+ ions were also measured to find the optimal dopant concentration. The highest intensity was observed at a 2.0 mol% concentration of Sm3+ ions at 604 nmwith concentration quenching occurring beyond this point. The CIE chromaticity coordinates for the different concentration phosphor were located in the orange-red region, indicating its characteristic light emission. So therefore, these results suggested that the synthesized reddish-orange light-emitting Ba3LaNa(PO4)3F: Sm3+prepared phosphor is promising for applications in white light-emitting diodes (WLEDs).